323 related articles for article (PubMed ID: 16283881)
21. A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's lines.
Gimelli G; Giorda R; Beri S; Gimelli S; Zuffardi O
Eur J Med Genet; 2007; 50(4):264-73. PubMed ID: 17567547
[TBL] [Abstract][Full Text] [Related]
22. A novel combined 15q11.2 duplication and a bisatellited supernumerary marker derived from chromosome 22: molecular characterization of the marker.
Dutta UR; Vempally S; Ranganath P; Dalal A
Gene; 2014 Apr; 539(1):162-7. PubMed ID: 24508374
[TBL] [Abstract][Full Text] [Related]
23. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
Tan YQ; Di YF; Song YZ; Cheng DH; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):392-6. PubMed ID: 17680527
[TBL] [Abstract][Full Text] [Related]
24. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
Koochek M; Harvard C; Hildebrand MJ; Van Allen M; Wingert H; Mickelson E; Holden JJ; Rajcan-Separovic E; Lewis ME
Clin Genet; 2006 Feb; 69(2):124-34. PubMed ID: 16433693
[TBL] [Abstract][Full Text] [Related]
25. Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.
Vermeesch JR; Melotte C; Salden I; Riegel M; Trifnov V; Polityko A; Rumyantseva N; Naumchik I; Starke H; Matthijs G; Schinzel A; Fryns JP; Liehr T
Eur J Med Genet; 2005; 48(3):319-27. PubMed ID: 16179227
[TBL] [Abstract][Full Text] [Related]
26. First prenatally detected small supernumerary neocentromeric derivative chromosome 13 resulting in a non-mosaic partial tetrasomy 13q.
Mascarenhas A; Matoso E; Saraiva J; Tönnies H; Gerlach A; Julião MJ; Melo JB; Carreira IM
Cytogenet Genome Res; 2008; 121(3-4):293-7. PubMed ID: 18758175
[TBL] [Abstract][Full Text] [Related]
27. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
Wyandt HE; Shim SH; Mark HF; Huang XL; Milunsky JM
Exp Mol Pathol; 2006 Jun; 80(3):262-6. PubMed ID: 16516886
[TBL] [Abstract][Full Text] [Related]
28. Mosaic tetrasomy 15q25-->qter in a newborn infant with multiple anomalies.
Van den Enden A; Verschraegen-Spae MR; Van Roy N; Decaluwe W; De Praeter C; Speleman F
Am J Med Genet; 1996 Jun; 63(3):482-5. PubMed ID: 8737657
[TBL] [Abstract][Full Text] [Related]
29. Coexistence of inverted Y, chromosome 15p+ and abnormal phenotype.
Acar H; Cora T; Erkul I
Genet Couns; 1999; 10(2):163-70. PubMed ID: 10422010
[TBL] [Abstract][Full Text] [Related]
30. Tetrasomy 15q25.2→qter identified with SNP microarray in a patient with multiple anomalies including complex cardiovascular malformation.
George-Abraham JK; Zimmerman SL; Hinton RB; Marino BS; Witte DP; Hopkin RJ
Am J Med Genet A; 2012 Aug; 158A(8):1971-6. PubMed ID: 22711292
[TBL] [Abstract][Full Text] [Related]
31. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
Melo JB; Matoso E; Polityko A; Saraiva J; Backx L; Vermeesch JR; Kosyakova N; Ewers E; Liehr T; Carreira IM
Cytogenet Genome Res; 2009; 125(2):109-14. PubMed ID: 19729913
[TBL] [Abstract][Full Text] [Related]
32. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
Mark HF; Wyandt H; Huang XL; Milunsky JM
Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
[TBL] [Abstract][Full Text] [Related]
33. An analphoid marker chromosome inv dup(15)(q26.1qter), detected during prenatal diagnosis and characterized via chromosome microdissection.
Mahjoubi F; Peters GB; Malafiej P; Shalhoub C; Turner A; Daniel A; Hill RJ
Cytogenet Genome Res; 2005; 109(4):485-90. PubMed ID: 15905642
[TBL] [Abstract][Full Text] [Related]
34. FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22).
Bartsch O; Rasi S; Hoffmann K; Blin N
Eur J Hum Genet; 2005 May; 13(5):592-8. PubMed ID: 15756300
[TBL] [Abstract][Full Text] [Related]
35. Molecular cytogenetic characterization of a metastatic lung sarcomatoid carcinoma: 9p23 neocentromere and 9p23-p24 amplification including JAK2 and JMJD2C.
Italiano A; Attias R; Aurias A; Pérot G; Burel-Vandenbos F; Otto J; Venissac N; Pedeutour F
Cancer Genet Cytogenet; 2006 Jun; 167(2):122-30. PubMed ID: 16737911
[TBL] [Abstract][Full Text] [Related]
36. Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridization.
Zhao J; Gordon PL; Wilroy RS; Martens PR; Tarleton J; Shulman LP; Simpson JL; Elias S; Tharapel AT
Am J Med Genet; 1995 May; 56(4):398-402. PubMed ID: 7604849
[TBL] [Abstract][Full Text] [Related]
37. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
[TBL] [Abstract][Full Text] [Related]
38. Supernumerary marker chromosomes detected in 100,000 prenatal diagnoses: molecular cytogenetic studies and clinical significance.
Huang B; Solomon S; Thangavelu M; Peters K; Bhatt S
Prenat Diagn; 2006 Dec; 26(12):1142-50. PubMed ID: 17009345
[TBL] [Abstract][Full Text] [Related]
39. A de novo 8q22.2-24.3 duplication in a patient with mild phenotype.
Concolino D; Iembo MA; Moricca MT; Rapsomaniki M; Marotta R; Galesi O; Fichera M; Romano C; Strisciuglio P
Eur J Med Genet; 2012 Jan; 55(1):67-70. PubMed ID: 21971480
[TBL] [Abstract][Full Text] [Related]
40. Neocentromere formation in a stable ring 1p32-p36.1 chromosome.
Slater HR; Nouri S; Earle E; Lo AW; Hale LG; Choo KH
J Med Genet; 1999 Dec; 36(12):914-8. PubMed ID: 10593999
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
